A model for the mechanism of strand passage by DNA gyrase

被引:127
作者
Kampranis, SC
Bates, AD
Maxwell, A [1 ]
机构
[1] Univ Leicester, Dept Biochem, Leicester LE1 7RH, Leics, England
[2] Univ Liverpool, Sch Biol Sci, Liverpool L69 7ZB, Merseyside, England
基金
英国惠康基金;
关键词
supercoiling; topoisomerase; energy coupling;
D O I
10.1073/pnas.96.15.8414
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mechanism of type II DNA topoisomerases involves the formation of an enzyme-operated gate in one double-stranded DNA segment and the passage of another segment through this gate. DNA gyrase is the only type II topoisomerase able to introduce negative supercoils into DNA a feature that requires the enzyme to dictate the directionality of strand passage. Although it is known that this is a consequence of the characteristic wrapping of DNA by gyrase, the detailed mechanism by which the transported DNA segment is captured and directed through the DNA gate is largely unknown. We have addressed this mechanism by probing the topology of the bound DNA segment at distinct steps of the catalytic cycle, We propose a model in which gyrase captures a contiguous DNA segment with high probability, irrespective of the superhelical density of the DNA substrate, setting up an equilibrium of the transported segment across the DNA gate. The overall efficiency of strand passage is determined by the position of this equilibrium, which depends on the superhelical density of the DNA substrate. This mechanism is concerted, in that capture of the transported segment by the ATP-operated clamp induces opening of the DNA. gate, which in turn stimulates ATP hydrolysis.
引用
收藏
页码:8414 / 8419
页数:6
相关论文
共 42 条
  • [1] THE 43-KILODALTON N-TERMINAL FRAGMENT OF THE DNA GYRASE-B PROTEIN HYDROLYZES ATP AND BINDS COUMARIN DRUGS
    ALI, JA
    JACKSON, AP
    HOWELLS, AJ
    MAXWELL, A
    [J]. BIOCHEMISTRY, 1993, 32 (10) : 2717 - 2724
  • [2] Bates A. D., 1993, DNA topology
  • [3] DNA GYRASE CAN SUPERCOIL DNA CIRCLES AS SMALL AS 174 BASE-PAIRS
    BATES, AD
    MAXWELL, A
    [J]. EMBO JOURNAL, 1989, 8 (06) : 1861 - 1866
  • [4] Energy coupling in Escherichia coli DNA gyrase: The relationship between nucleotide binding, strand passage, and DNA supercoiling
    Bates, AD
    ODea, MH
    Gellert, M
    [J]. BIOCHEMISTRY, 1996, 35 (05) : 1408 - 1416
  • [5] Structure and mechanism of DNA topoisomerase II
    Berger, JM
    Gamblin, SJ
    Harrison, SC
    Wang, JC
    [J]. NATURE, 1996, 379 (6562) : 225 - 232
  • [6] Crystal structure of the breakage-reunion domain of DNA gyrase
    Cabral, JHM
    Jackson, AP
    Smith, CV
    Shikotra, N
    Maxwell, A
    Liddington, RC
    [J]. NATURE, 1997, 388 (6645) : 903 - 906
  • [7] Caron P R, 1994, Adv Pharmacol, V29B, P271
  • [8] The interaction of the F plasmid killer protein, CcdB, with DNA gyrase: Induction of DNA cleavage and blocking of transcription
    Critchlow, SE
    ODea, MH
    Howells, AJ
    Couturier, M
    Gellert, M
    Maxwell, A
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1997, 273 (04) : 826 - 839
  • [9] DNA cleavage is not required for the binding of quinolone drugs to the DNA Gyrase - DNA complex
    Critchlow, SE
    Maxwell, A
    [J]. BIOCHEMISTRY, 1996, 35 (23) : 7387 - 7393
  • [10] Exploiting nucleotide thiophosphates to probe mechanistic aspects of Escherichia coli DNA gyrase
    Cullis, PM
    Maxwell, A
    Weiner, DP
    [J]. BIOCHEMISTRY, 1997, 36 (20) : 6059 - 6068